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Determinants of Lipid Domain Size

Lipid domains less than 200 nm in size may form a scaffold, enabling the concerted function of plasma membrane proteins. The size-regulating mechanism is under debate. We tested the hypotheses that large values of spontaneous monolayer curvature are incompatible with micrometer-sized domains. Here,...

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Autores principales: Saitov, Ali, Kalutsky, Maksim A., Galimzyanov, Timur R., Glasnov, Toma, Horner, Andreas, Akimov, Sergey A., Pohl, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8998648/
https://www.ncbi.nlm.nih.gov/pubmed/35408861
http://dx.doi.org/10.3390/ijms23073502
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author Saitov, Ali
Kalutsky, Maksim A.
Galimzyanov, Timur R.
Glasnov, Toma
Horner, Andreas
Akimov, Sergey A.
Pohl, Peter
author_facet Saitov, Ali
Kalutsky, Maksim A.
Galimzyanov, Timur R.
Glasnov, Toma
Horner, Andreas
Akimov, Sergey A.
Pohl, Peter
author_sort Saitov, Ali
collection PubMed
description Lipid domains less than 200 nm in size may form a scaffold, enabling the concerted function of plasma membrane proteins. The size-regulating mechanism is under debate. We tested the hypotheses that large values of spontaneous monolayer curvature are incompatible with micrometer-sized domains. Here, we used the transition of photoswitchable lipids from their cylindrical conformation to a conical conformation to increase the negative curvature of a bilayer-forming lipid mixture. In contrast to the hypothesis, pre-existing micrometer-sized domains did not dissipate in our planar bilayers, as indicated by fluorescence images and domain mobility measurements. Elasticity theory supports the observation by predicting the zero free energy gain for splitting large domains into smaller ones. It also indicates an alternative size-determining mechanism: The cone-shaped photolipids reduce the line tension associated with lipid deformations at the phase boundary and thus slow down the kinetics of domain fusion. The competing influence of two approaching domains on the deformation of the intervening lipids is responsible for the kinetic fusion trap. Our experiments indicate that the resulting local energy barrier may restrict the domain size in a dynamic system.
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spelling pubmed-89986482022-04-12 Determinants of Lipid Domain Size Saitov, Ali Kalutsky, Maksim A. Galimzyanov, Timur R. Glasnov, Toma Horner, Andreas Akimov, Sergey A. Pohl, Peter Int J Mol Sci Article Lipid domains less than 200 nm in size may form a scaffold, enabling the concerted function of plasma membrane proteins. The size-regulating mechanism is under debate. We tested the hypotheses that large values of spontaneous monolayer curvature are incompatible with micrometer-sized domains. Here, we used the transition of photoswitchable lipids from their cylindrical conformation to a conical conformation to increase the negative curvature of a bilayer-forming lipid mixture. In contrast to the hypothesis, pre-existing micrometer-sized domains did not dissipate in our planar bilayers, as indicated by fluorescence images and domain mobility measurements. Elasticity theory supports the observation by predicting the zero free energy gain for splitting large domains into smaller ones. It also indicates an alternative size-determining mechanism: The cone-shaped photolipids reduce the line tension associated with lipid deformations at the phase boundary and thus slow down the kinetics of domain fusion. The competing influence of two approaching domains on the deformation of the intervening lipids is responsible for the kinetic fusion trap. Our experiments indicate that the resulting local energy barrier may restrict the domain size in a dynamic system. MDPI 2022-03-23 /pmc/articles/PMC8998648/ /pubmed/35408861 http://dx.doi.org/10.3390/ijms23073502 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Saitov, Ali
Kalutsky, Maksim A.
Galimzyanov, Timur R.
Glasnov, Toma
Horner, Andreas
Akimov, Sergey A.
Pohl, Peter
Determinants of Lipid Domain Size
title Determinants of Lipid Domain Size
title_full Determinants of Lipid Domain Size
title_fullStr Determinants of Lipid Domain Size
title_full_unstemmed Determinants of Lipid Domain Size
title_short Determinants of Lipid Domain Size
title_sort determinants of lipid domain size
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8998648/
https://www.ncbi.nlm.nih.gov/pubmed/35408861
http://dx.doi.org/10.3390/ijms23073502
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